Canonical Allele Identifier: CA412952896

Gene: FOXP3

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.49257474G>A , CM000685.2:g.49257474G>A	GRCh38
NC_000023.10:g.49113931G>A , CM000685.1:g.49113931G>A	GRCh37
NC_000023.9:g.49000875G>A	NCBI36
NG_007392.1:g.12358C>T , LRG_62:g.12358C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_014009.4:c.407C>T MANE Select	NP_054728.2:p.Thr136Ile
ENST00000376207.10:c.407C>T MANE Select	ENSP00000365380.4:p.Thr136Ile
NM_001114377.1:c.302C>T	NP_001107849.1:p.Thr101Ile
NM_001114377.2:c.302C>T	NP_001107849.1:p.Thr101Ile
NM_014009.3:c.407C>T , LRG_62t1:c.407C>T	NP_054728.2:p.Thr136Ile
ENST00000376197.1:c.257C>T	ENSP00000365369.1:p.Thr86Ile
ENST00000376199.6:c.302C>T	ENSP00000365372.2:p.Thr101Ile
ENST00000376199.7:c.302C>T	ENSP00000365372.2:p.Thr101Ile
ENST00000376207.8:c.407C>T	ENSP00000365380.4:p.Thr136Ile
ENST00000455775.6:c.407C>T	ENSP00000396415.3:p.Thr136Ile
ENST00000455775.7:c.407C>T	ENSP00000396415.3:p.Thr136Ile
ENST00000518685.5:c.302C>T	ENSP00000428952.1:p.Thr101Ile
ENST00000518685.6:c.407C>T	ENSP00000428952.2:p.Thr136Ile
ENST00000557224.5:c.302C>T	ENSP00000451208.1:p.Thr101Ile
ENST00000557224.6:c.302C>T	ENSP00000451208.1:p.Thr101Ile
ENST00000651307.1:c.407C>T	ENSP00000498454.1:p.Thr136Ile
ENST00000652559.1:c.260C>T	ENSP00000498236.1:p.Thr87Ile
XM_006724533.2:c.407C>T	XP_006724596.2:p.Thr136Ile
XM_011543915.1:c.626C>T	XP_011542217.1:p.Thr209Ile
XM_011543916.1:c.626C>T	XP_011542218.1:p.Thr209Ile
XM_011543917.1:c.425C>T	XP_011542219.1:p.Thr142Ile
XM_011543918.1:c.662C>T	XP_011542220.1:p.Thr221Ile
XM_011543919.1:c.626C>T	XP_011542221.1:p.Thr209Ile
XM_017029567.1:c.353C>T	XP_016885056.1:p.Thr118Ile